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Diseases
Genes (441)
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ASL
Argininosuccinic Aciduria
MYH9
Arterial Tortuosity Syndrome
Myh9-Related Disease
TTPA
Familial Isolated Vitamin E Deficiency
FKTN
Fukuyama Congenital Muscular Dystrophy
TNNI2
Sheldon-Hall Syndrome
PMM2
Pmm2 Deficiency
SLC2A10
Hiatal Hernia
Arterial Tortuosity Syndrome
PQBP1
Renpenning's Syndrome
MYH3
Sheldon-Hall Syndrome
IFIH1
Singleton Merten Syndrome
TPM2
Sheldon-Hall Syndrome
TNNT3
Sheldon-Hall Syndrome
FKRP
Fukuyama Congenital Muscular Dystrophy
RB1
Pinealoblastoma
Trilateral Retinoblastoma
COMT
Tmj Disorders
DAG1
Fukuyama Congenital Muscular Dystrophy
THAS
Hernia
COL1A1
Hernia
Hiatal Hernia
COL3A1
Hernia
Hiatal Hernia
Uterine Rupture
DDX58
Singleton Merten Syndrome